{{Rsnum
|rsid=121909137
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CLCNKA
|position=16024773
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLCNKA
}}{{omim
|id=602024
|rsnum=121909137
|variant=0001
}}{{ClinVar
|rsid=121909137
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=16024773
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060080a05000002110100
|GENEINFO=CLCNKA:1187
|GENE_NAME=CLCNKA
|GENE_ID=1187
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.16024773G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001257139.1:c.229+845G>C; NM_004070.3:c.240G>C; 602024.0001
|CLNSIG=5
|CLNCUI=CN035435
|CLNDBN=Bartter syndrome, type 4b
|Disease=Bartter syndrome
|CLNACC=RCV000008027.2
|Tags=PM;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2751312:613090
}}